| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30698037-30698235 | Common:1; Rare:102 | ||||
| chr16:30698434-30698647 | Common:1; Rare:83 | ||||
| chr16:30698969-30699394 | Rare:120; Clinvar (benign):1 | ||||
| chr16:30748125-30748462 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30761443-30761600 | Rare:63 | ||||
| chr16:30762090-30762333 | Common:3; Rare:86 | ||||
| chr16:30787118-30787302 | Rare:33 | ||||
| chr16:30893960-30894275 | Common:5; Rare:84 | ||||
| chr16:30923236-30923588 | Common:1; Rare:86 | ||||
| chr16:31073722-31073848 | Rare:39 | ||||
| chr16:31074187-31074457 | Common:1; Rare:75 | ||||
| chr16:31074631-31074848 | Common:2; Rare:44 | ||||
| chr16:31094573-31095050 | Common:1; Rare:147; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108283-31108471 | Rare:42 | ||||
| chr16:31179827-31180165 | Common:2; Rare:133; Clinvar:1; Clinvar (benign):1 |